Leanne De Kock
Ottawa, ON, Canada
Last Updated: 09/26/2026
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Found 48 publications
A Mosaic Hotspot PLCD1 Variant, Detectable in Blood-Derived DNA, Associated With Nevus Trichilemmocysticus.
Journal: American journal of medical genetics. Part A
Published: January 31, 2025
Molecular characterization of 13 patients with PIK3CA-related overgrowth spectrum using a targeted deep sequencing approach.
Journal: American journal of medical genetics. Part A
Published: September 29, 2023
Reclassification of two germline DICER1 splicing variants leads to DICER1 syndrome diagnosis.
Journal: Familial cancer
Published: February 09, 2023
Bridging clinical care and research in Ontario, Canada: Maximizing diagnoses from reanalysis of clinical exome sequencing data.
Journal: Clinical genetics
Published: September 25, 2022
Long-term tumour dormancy in a BRCA1 heterozygote.
Journal: Journal of medical genetics
Published: October 13, 2021
An Unusual Enteric Yolk Sac Tumor: First Report of an Ovarian Germ Cell Tumor Associated With a Germline Pathogenic Variant in DICER1.
Journal: International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists
Published: August 12, 2021
Likely foregut endoderm origin for a postzygotic mutation affecting the RNase IIIb domain of DICER1.
Likely foregut endoderm origin for a postzygotic mutation affecting the RNase IIIb domain of DICER1.
Journal: Journal of medical genetics
Published: March 31, 2021
Embryonal rhabdomyosarcoma of the uterine corpus: a clinicopathological and molecular analysis of 21 cases highlighting a frequent association with DICER1 mutations.
Journal: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
Published: December 22, 2020
Molecular characterization of DICER1-mutated pituitary blastoma.
Journal: Acta neuropathologica
Published: December 22, 2020
Endometrial Stem/Progenitor cell (ES/PC) Marker Expression Profile in Adenosarcoma and Endometrial Stromal Sarcoma.
Journal: Cancer treatment and research communications
Published: October 15, 2020
A complex DICER1 syndrome phenotype associated with a germline pathogenic variant affecting the RNase IIIa domain of DICER1.
Journal: Journal of medical genetics
Published: August 05, 2020
Last Updated: 09/26/2026